Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/–KTS splice isoforms

By Klamt B.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 709-714

Oxford University Press

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Conserved use of a non-canonical 5′ splice site (/GA) in alternative splicing by fibroblast growth factor receptors 1, 2 and 3

By Twigg S.R.F.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 685-691

Oxford University Press

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Bare-1 insertion site preferences and evolutionary conservation of RNA and cDNA processing sites

By Suoniemi A.   Schmidt D.   Schulman A.H.  

Genetica, Vol. 100, Iss. 1-3, 1997-01 ,pp. : 219-230

Springer Publishing Company

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A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene ( MeCP2 ) suggests a regulatory role in gene expression

By Coy Johannes F.  

Human Molecular Genetics, Vol. 8, Iss. 7, 1999-07 ,pp. : 1253-1262

Oxford University Press

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Cyclin D1 splice variant and risk for non-Hodgkin lymphoma

By Wang Sophia   Cozen Wendy   Severson Richard   Hartge Patricia   Cerhan James   Davis Scott   Welch Robert   Rothman Nathaniel   Chanock Stephen  

Human Genetics, Vol. 120, Iss. 2, 2006-09 ,pp. : 297-300

Springer Publishing Company

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